Lead Recruiter – Regulatory & Clinical (CRO/Pharma)

1 day, 10 hours ago
Welo Global

Welo Global

Welo Global specializes in providing enterprise localization, AI training data, and multilingual content solutions, leveraging a portfolio of specialized global brands to meet diverse customer needs in the AI and language services industry.

Professional Services
Founded 1997

Description

  • Lead the full recruitment lifecycle for specialized Regulatory and Clinical roles globally, including Clinical Trial Management, Regulatory Affairs, Pharmacovigilance, Medical Writing, and related disciplines.
  • Drive candidate attraction through specialist channels such as clinical trial registries, professional associations, and targeted direct sourcing.
  • Create and apply assessment frameworks to evaluate candidates and freelancers against technical competency frameworks and project-specific requirements.
  • Manage and guide a small team of recruiters and partner management professionals through daily coaching, prioritization, and delivery oversight.
  • Monitor hiring pipelines, identify risks early, and adjust recruitment approaches to protect delivery against shifting project demands.
  • Build trusted relationships with cross-functional stakeholders across regions and translate hiring needs into precise recruitment briefs.
  • Maintain and optimize Lever ATS workflows, reporting dashboards, structured interview processes, and partner management integrations.
  • Provide regular reporting and insights on time-to-fill, pipeline health, salary benchmarking, market trends, and team performance.
  • Lead vendor management activities, including partner accountability, issue resolution, escalation handling, and service quality oversight.
  • Oversee specialist and freelance vendor pricing to ensure competitive, commercially sound rate structures across markets.

Requirements

  • Minimum 7 years of talent acquisition experience, including at least 3 years in Life Sciences, CRO, and/or Pharma.
  • Demonstrable recruitment experience in Clinical Trials, Regulatory Affairs, and/or Pharmacovigilance.
  • Extensive knowledge of Life Sciences recruitment, including GCP, ICH frameworks, and regulatory submission processes.
  • Experience creating and deploying assessment frameworks for technical and competency-based evaluation.
  • Advanced working knowledge of Lever ATS, including pipeline automation, structured reporting, workflow configuration, and integrations.
  • Experience managing external partner relationships, including negotiation, relationship management, and strategic evaluation.
  • Proven experience managing or mentoring a small team and developing colleagues in day-to-day delivery.
  • Strong stakeholder management skills across regions, functions, and cultural contexts.
  • Familiarity with client audits and supporting audit readiness in a CRO or Pharma recruitment context.
  • Preferred experience with recruitment automation and AI-assisted sourcing tools, freelance/contractor talent models, multilingual hiring, and workflow automation tools.

Interested in this position?

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